Warfarin Time in Therapeutic INR Range and Direct Oral Anticoagulant Adherence for Venous Thromboembolism Across the Spectrum of Weight and Body Mass Index: Findings from Veterans Health Administration

Author:

Din Natasha12,Fan Jun1,Schmitt Susan1,Guo Jennifer D.3,Hlavacek Patrick4,Pundi Krishna5,Russ Cristina4,Emir Birol4,Turakhia Mintu P.125,Perino Alexander C.125ORCID

Affiliation:

1. Veterans Affairs Palo Alto Health Care System, Palo Alto, CA, USA

2. Center for Digital Health, Stanford University School of Medicine, Stanford, CA, USA

3. Bristol Myers Squibb, Lawrenceville, NJ, USA former employee at the time the study was conducted

4. Pfizer, New York, NY, USA

5. Department of Medicine, Stanford University School of Medicine, Stanford, CA, USA

Abstract

The evidence of direct oral anticoagulants (DOACs) usage for venous thromboembolism (VTE) in patients at extremes of body weight or mass index is limited. In such situations, warfarin may be more frequently used. We investigated warfarin time in the therapeutic international normalized ratio range (TTR) and DOAC adherence based on the calculated proportion of days covered (PDC) by pill coverage from a DOAC prescription in patients with VTE across all body sizes. Using data from the Veterans Health Administration (VA), we identified first-time patients with VTE between 2013 and 2018 treated with warfarin or DOACs. We analyzed 28,245 patients with warfarin TTR (N  =  10,167) or DOAC PDC(N  =  18,078). For warfarin-treated patients after index VTE, mean TTR was lower over shorter treatment durations (TTR 30 vs TTR 180 [mean  ±  SD]: 43.8% ± 33.5% vs 58.8% ± 23.5%). Mean TTR over 180 days after VTE was lowest for patients <60 kg (TTR 180 [mean  ±  SD]: <60kg: 49.3% ± 24.2% vs ≥60 to <100 kg: 57.8% ± 23.4%; P < .0001). For DOAC-treated patients over 180 days after index VTE, mean PDC was lowest for patients <60 kg (PDC 180 [mean  ±  SD]: < 60kg: 76.9% ± 33.2% vs ≥ 60 to <100 kg: 83.6% ± 27.7%; P < .0001). Most DOAC-treated patients attained sufficient adherence across the body size spectrum while warfarin-treated patients <60kg were at risk for low TTR.

Funder

Bristol Myers Squibb-Pfizer Alliance

Publisher

SAGE Publications

Subject

Hematology,General Medicine

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